Canonical Allele Identifier: CA354745190

Gene: STAG1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.136604467T>C , CM000665.2:g.136604467T>C	GRCh38
NC_000003.11:g.136323309T>C , CM000665.1:g.136323309T>C	GRCh37
NC_000003.10:g.137805999T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000383202.7:c.139A>G MANE Select	ENSP00000372689.2:p.Asn47Asp
ENST00000236698.9:c.139A>G	ENSP00000236698.5:p.Asn47Asp
ENST00000383202.6:c.139A>G	ENSP00000372689.2:p.Asn47Asp
ENST00000434713.6:c.-540A>G	ENSP00000404396.2:n.-540A>G
ENST00000462818.1:n.7A>G
ENST00000480733.1:c.139A>G	ENSP00000420789.1:p.Asn47Asp
ENST00000483235.5:c.139A>G	ENSP00000419093.1:p.Asn47Asp
ENST00000487065.5:c.139A>G	ENSP00000418472.1:p.Asn47Asp
ENST00000629124.2:c.139A>G	ENSP00000486745.1:p.Asn47Asp
NM_005862.2:c.139A>G	NP_005853.2:p.Asn47Asp
XM_011512329.1:c.-503A>G	XP_011510631.1:n.-503A>G
XM_011512331.1:c.-398A>G	XP_011510633.1:n.-398A>G
XM_011512329.2:c.-503A>G	XP_011510631.1:n.-503A>G
XM_011512331.2:c.-398A>G	XP_011510633.1:n.-398A>G
XM_017005523.1:c.-176A>G	XP_016861012.1:n.-176A>G
XM_017005524.2:c.-708A>G	XP_016861013.1:n.-708A>G
XR_001739978.1:n.417A>G
NM_005862.3:c.139A>G MANE Select	NP_005853.2:p.Asn47Asp